A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819058



Internal ID21264396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125577589..125577589hg38UCSC Ensembl
chr9:128339868..128339868hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13700037
Samples
Known GenesMAPKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819058
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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